meddevicedb.com FDA Device Reference

UV Radiation Treatment System

K191571 Class II Traditional
Decision Date
2020-02-06
Sponsor / Applicant
Xuzhou Yongkang Electronic Science Technology Co., Ltd.

Technical Specification

510(k) Submission ID K191571
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2020-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UV Radiation Treatment System received FDA 510(k) clearance under submission number K191571, sponsored by Xuzhou Yongkang Electronic Science Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.